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CTNM News

Contineum Therapeutics Q1 Financial Results

May 05 2026seekingalpha

Contineum Therapeutics Reports Positive Phase 1b Trial Results for PIPE-791

May 01 2026NASDAQ.COM

Contineum Therapeutics Reports Q4 Earnings and Public Offering

Mar 05 2026seekingalpha

Moderna Inc (MRNA) Projects $1.9 Billion Revenue for 2025, Shares Surge 12.8%

Jan 13 2026Benzinga

Contineum Therapeutics Prices Upsized Offering of 7.35M Shares at $12.25, Raising $90M

Dec 12 2025Newsfilter

Contineum Therapeutics Prices Upsized Offering of 7.35M Shares at $12.25, Raising $90M

Dec 12 2025Businesswire

Contineum Therapeutics Launches $75 Million Public Offering

Dec 11 2025Newsfilter

Contineum Stock Declines Following Unsuccessful Phase 2 PIPE-307 Trial for Multiple Sclerosis Efficacy

Nov 21 2025Yahoo Finance

CTNM Events

05/05 17:00
Contineum Cash Resources Sufficient Through Mid-2029
Cash, cash equivalents and marketable securities were $246.3 million as of March 31, 2026. Contineum believes its cash resources are sufficient to fund its planned operations through mid-2029. "We're excited to have recently shared positive topline results from our chronic pain trial," said Carmine Stengone, CEO, Contineum Therapeutics. "We continue to steadily enroll PROPEL-IPF, a global Phase 2 trial evaluating PIPE-791 for the treatment of patients with idiopathic pulmonary fibrosis (IPF). With a projected cash runway that extends through mid-2029, which is approximately one year past the estimated completion of our IPF trial, we are maintaining a disciplined approach to capital allocation that prioritizes our lead clinical indication, while thoughtfully considering the advancement of other programs."
04/30 16:30
Contineum Therapeutics Reports Positive Data from PIPE-791 Trial
Contineum Therapeutics reported positive topline data from its exploratory Phase 1b trial of PIPE-791, a potentially best-in-class selective antagonist of the lysophosphatidic acid 1 (LPA1) receptor, for the non-opioid treatment of chronic osteoarthritis pain or chronic low back pain. The randomized, double-blind, placebo-controlled, 4-week, crossover trial enrolled 43 patients (23 COAP and 20 CLBP). The trial design incorporated a washout period for patients prior to the first 4-week treatment period (TP1), after which patients crossed over immediately into a second 4-week treatment period (TP2) without an intervening PIPE-791 washout. PIPE-791 was administered orally at 10mg once-daily.

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